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Medline MDR107002LRecalls & reported problems

Medline Industries, Inc. · BED, SEMI ELECTRIC, MEDLITE · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
31
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 31 adverse event reports that list this exact device (DI 40080196294320), received between May 6, 2026 and Sep 30, 2026 — classified as 31 malfunctions.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (16 reports).

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 4 reportsJun 2026: 2 reportsJul 2026: 10 reportsAug 2026: 2 reportsSep 2026: 13 reportsOct 2026: 0 reports20242025202613
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Nov 26, 2025Open, Classified

    Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.

    Z-1012-2026 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Device problems

  • Electrical /Electronic Property Problem16
  • Fracture4
  • Mechanical Problem4
  • Loose or Intermittent Connection2
  • Complete Loss of Power1
  • Crack1
  • Insufficient Device Problem Information1
  • Key or Button Unresponsive/not Working1

Patient problems

  • No Clinical Signs, Symptoms or Conditions31

Recent adverse event reports

The 25 most recent of 31 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 30, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50948668 ↗
  • MalfunctionSep 30, 2026Electrical /Electronic Property Problem

    It was reported that "the pendant is not working and there is no function to the bed" and "wires are exposed on the pendant."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50945341 ↗
  • MalfunctionSep 29, 2026Fracture

    It was reported that "Patient heard a pop noise when trying to raise head of bed, the motor snapped."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50936930 ↗
  • MalfunctionSep 29, 2026Crack

    It was reported that "The frame of the bed has been cracked."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50931460 ↗
  • MalfunctionSep 28, 2026Fracture

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50918632 ↗
  • MalfunctionSep 28, 2026Fracture

    It was reported that "this drivearm came apart during the bed test after it was cleaned. It doesn't want to go back together.".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50917349 ↗
  • MalfunctionSep 24, 2026Loose or Intermittent Connection

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50885239 ↗
  • MalfunctionSep 23, 2026Electrical /Electronic Property Problem

    It was reported that "for both beds all functions of the bed work besides the head/foot section of the bed will not go up or down." Customer stated that "the hand remote is not working and all they could hear is a \"humming or clicking noise\" and the bed does not move."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50873235 ↗
  • MalfunctionSep 23, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50873177 ↗
  • MalfunctionSep 23, 2026Material Frayed; Material Split, Cut or Torn

    It was reported that "Bed remote and electrical cord got pinched in between bed. Both still work but there is tape over it."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50871512 ↗
  • MalfunctionSep 22, 2026Fracture

    It was reported that "The head shaft broke off that comes out of the actuator."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50857612 ↗
  • MalfunctionSep 22, 2026Electrical /Electronic Property Problem

    It was reported that Bed foot actuator quit working. It makes a noise but nothing happens.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50855998 ↗
  • MalfunctionSep 21, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50842956 ↗
  • MalfunctionAug 24, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50418820 ↗
  • MalfunctionAug 6, 2026Mechanical Problem

    It was reported that foot spring would not raise. Took motor off and the bar that raises the foot section came loose from the motor.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50161339 ↗
  • MalfunctionJul 27, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50007957 ↗
  • MalfunctionJul 27, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50007705 ↗
  • MalfunctionJul 27, 2026Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50002107 ↗
  • MalfunctionJul 27, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50001608 ↗
  • MalfunctionJul 27, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50001579 ↗
  • MalfunctionJul 27, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50000819 ↗
  • MalfunctionJul 27, 2026Key or Button Unresponsive/not Working

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50000812 ↗
  • MalfunctionJul 27, 2026Electrical /Electronic Property Problem; Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50000474 ↗
  • MalfunctionJul 27, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50000116 ↗
  • MalfunctionJul 27, 2026Electrical /Electronic Property Problem

    It was reported that the foot spring does not respond at all.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50000045 ↗

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Sources and updates

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